The hypothalamic–pituitary–thyroid axis is intact in male Irs4 knockout mice
Objective: Loss of function mutations in the insulin receptor substrate 4 (IRS4) gene cause a rare form of X-linked congenital central hypothyroidism in boys and men. Affected individuals show decreased thyroid-stimulating hormone (TSH) secretion. Members of the IRS family canonically act as scaffol...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Bioscientifica
2024-02-01
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Series: | European Thyroid Journal |
Subjects: | |
Online Access: | https://etj.bioscientifica.com/view/journals/etj/13/1/ETJ-23-0054.xml |